Delta 5-sterole en provitamiene D met vertakte sykettings

Daniel Francois Louw

Delta 5-sterole en provitamiene D met vertakte sykettings

Daniel Francois Louw

Faculty of Science and Engineering

Research output: Thesis › Thesis fully internal (DIV)

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Abstract

Windaus, Lettré and Schenk synthesised 7-dehydrocholesterol (I) by pyrolysis of the dibenzoate of 7-hydroxycholestrol. On comparing this syntetic provitamin D with ergosterol (II) they came to the conclusion that a number of steroids differing in the degree of unsaturation and in the length of the side chain, but having the same system of conjugated double bonds in ring B of the nucleus, would be convertible to antirachitic substances (vitamins D) by irradiation with ultra-violet light. ... Zie: Summary

Original language	Dutch
Qualification	Doctor of Philosophy
Supervisors/Advisors	Backer, H.J., Supervisor, External person
Award date	16-Sept-1953
Place of Publication	Groningen
Publisher	s.n.
Publication status	Published - 1953

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title = "Delta 5-sterole en provitamiene D met vertakte sykettings",

abstract = "Windaus, Lettr{\'e} and Schenk synthesised 7-dehydrocholesterol (I) by pyrolysis of the dibenzoate of 7-hydroxycholestrol. On comparing this syntetic provitamin D with ergosterol (II) they came to the conclusion that a number of steroids differing in the degree of unsaturation and in the length of the side chain, but having the same system of conjugated double bonds in ring B of the nucleus, would be convertible to antirachitic substances (vitamins D) by irradiation with ultra-violet light. ... Zie: Summary",

author = "Louw, {Daniel Francois}",

note = "Relation: http://www.rug.nl/ Rights: University of Groningen",

year = "1953",

language = "Dutch",

publisher = "s.n.",

}

TY - BOOK

T1 - Delta 5-sterole en provitamiene D met vertakte sykettings

AU - Louw, Daniel Francois

N1 - Relation: http://www.rug.nl/ Rights: University of Groningen

PY - 1953

Y1 - 1953

N2 - Windaus, Lettré and Schenk synthesised 7-dehydrocholesterol (I) by pyrolysis of the dibenzoate of 7-hydroxycholestrol. On comparing this syntetic provitamin D with ergosterol (II) they came to the conclusion that a number of steroids differing in the degree of unsaturation and in the length of the side chain, but having the same system of conjugated double bonds in ring B of the nucleus, would be convertible to antirachitic substances (vitamins D) by irradiation with ultra-violet light. ... Zie: Summary

AB - Windaus, Lettré and Schenk synthesised 7-dehydrocholesterol (I) by pyrolysis of the dibenzoate of 7-hydroxycholestrol. On comparing this syntetic provitamin D with ergosterol (II) they came to the conclusion that a number of steroids differing in the degree of unsaturation and in the length of the side chain, but having the same system of conjugated double bonds in ring B of the nucleus, would be convertible to antirachitic substances (vitamins D) by irradiation with ultra-violet light. ... Zie: Summary

M3 - Thesis fully internal (DIV)

PB - s.n.

CY - Groningen

ER -